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Australian Systematic Botany Australian Systematic Botany Society
Taxonomy, biogeography and evolution of plants
RESEARCH ARTICLE

Reliable analysis of volatile compounds from small samples of Eucalyptus magnificata (Myrtaceae)

Timothy L. Collins orcid.org/0000-0002-4055-9381 A C , Rose L. Andrew A , Ben W. Greatrex B and Jeremy J. Bruhl orcid.org/0000-0001-9112-4436 A
+ Author Affiliations
- Author Affiliations

A School of Environmental and Rural Science, University of New England, Trevenna Road, Armidale, NSW 2351, Australia.

B School of Science and Technology, University of New England, Trevenna Road, Armidale, NSW 2351, Australia.

C Corresponding author. Email: tcollins@myune.edu.au

Australian Systematic Botany 31(3) 232-240 https://doi.org/10.1071/SB18005
Submitted: 12 February 2018  Accepted: 25 May 2018   Published: 9 July 2018

Abstract

Phytochemistry is a source of data for plant systematics. This tool has much more value if herbarium specimens can be used without major damage and if results are comparable with fresh samples. A modified method for the solvent extraction of eucalypt leaf oils for phytochemical analysis and chemotaxonomy studies, including historical herbarium samples by gas chromatography–mass spectrometry (GC-MS), has been statistically assessed using Eucalyptus magnificata L.A.S.Johnson & K.D.Hill leaves. Leaf sample size was reduced by a factor of 250 to minimise damage to herbarium specimens, reduce solvent volume and simplify preparation of solvent extract before analysis. Leaf sampling treatments assessed the effects of the number of leaves and post-harvest air-drying on variation in components in the solvent extract. The results showed no statistically significant effect of leaf mass or the number of leaves used in GC-MS analyses on the precision of the measurements, but a significant difference among treatments for some oil constituents, particularly 1,8-cineole. Most differences in terpenoid concentration were due to variation among plants rather than extraction treatments. Extracts from air-dried herbarium leaves up to 44 years old were directly comparable with those from fresh leaves. Solvent extraction in 2 mL GC-MS vials of ~0.5 cm2 (16 mg) of leaf material, using fragments of fresh or air-dried leaves, drastically reduced sample and solvent volumes and showed that sampling from E. magnificata herbarium specimens for chemotaxonomy and chemotyping is a valid method, enabling broader sampling with much lower costs than for traditional fieldwork collections.

Additional keywords: chemotaxonomy, cineole, GC-MS, herbarium, herbarium specimens, Myrtaceae, solvent extraction, taxonomy, terpenes.


References

Adams RP (Ed.) (2007) ‘Identification of Essential Oil Components by Gas Chromatography/Mass Spectrometry.’ (Allured Publishing Corporation: Carol Stream, IL, USA)

Ammon DG, Barton AFM, Clarke DA, Tjandra J (1985) Rapid and accurate determination of terpenes in the leaves of Eucalyptus species. Analyst 110, 921–924.
Rapid and accurate determination of terpenes in the leaves of Eucalyptus species.Crossref | GoogleScholarGoogle Scholar |

Andreasen K, Manktelow M, Razafimandimbison SG (2009) Successful DNA amplification of a more than 200-year-old herbarium specimen: recovering genetic material from the Linnaean era. Taxon 58, 959–962.

Andrew RL, Keszei A, Foley WJ (2013) Intensive sampling identifies previously unknown chemotypes, population divergence and biosynthetic connections among terpenoids in Eucalyptus tricarpa. Phytochemistry 94, 148–158.
Intensive sampling identifies previously unknown chemotypes, population divergence and biosynthetic connections among terpenoids in Eucalyptus tricarpa.Crossref | GoogleScholarGoogle Scholar |

Baker GR, Lowe RF, Southwell IA (2000) Comparison of oil recovered from tea tree leaf by ethanol extraction and steam distillation. Journal of Agricultural and Food Chemistry 48, 4041–4043.
Comparison of oil recovered from tea tree leaf by ethanol extraction and steam distillation.Crossref | GoogleScholarGoogle Scholar |

Barton AFM, Tjandra J, Nicholas PG (1989) Chemical evaluation of volatile oils in Eucalyptus species. Journal of Agricultural and Food Chemistry 37, 1253–1257.
Chemical evaluation of volatile oils in Eucalyptus species.Crossref | GoogleScholarGoogle Scholar |

Beck JB, Semple JC (2015) Next-generation sampling: pairing genomics with herbarium specimens provides species-level signal in Solidago (Asteraceae). Applications in Plant Sciences 3, 1500014
Next-generation sampling: pairing genomics with herbarium specimens provides species-level signal in Solidago (Asteraceae).Crossref | GoogleScholarGoogle Scholar |

Boland DJ, Brophy JJ, House APN (1991) ‘Eucalyptus Leaf Oils: Use, Chemistry, Distillation and Marketing.’ (Inkata Press: Canberra, ACT, Australia)

Brooker MIH, Barton AFM, Rockel BA, Tjandra J (1988) The cineole content and taxonomy of Eucalyptus kochii Maiden&Blakely and E. plenissima (Gardner) Brooker, with an appendix establishing these two taxa as subspecies. Australian Journal of Botany 36, 119–129.
The cineole content and taxonomy of Eucalyptus kochii Maiden&Blakely and E. plenissima (Gardner) Brooker, with an appendix establishing these two taxa as subspecies.Crossref | GoogleScholarGoogle Scholar |

Brophy JJ, Forster PI, Goldsack RJ, Hibbert DB, Punruckvong A (2009) Essential oil variation in Eucalyptus crebra, E. melanophloia (Myrtaceae) and their hybrids. Australian Journal of Botany 57, 425–431.
Essential oil variation in Eucalyptus crebra, E. melanophloia (Myrtaceae) and their hybrids.Crossref | GoogleScholarGoogle Scholar |

Cousins DJ (1995) Review of aromatic and medicinal plants. CAB Abstracts 1, 1–60.

Dowell A, Sadgrove NJ, Telford IR, Greatrex B, Jones GL (2013) Dihydrotagetone an unusual fruity ketone is found in enantiopure and enantioenriched forms in additional Australian native taxa of Phebalium (Rutaceae: Boronieae). Natural Product Communications 8, 737–740.

Dunlop PJ, Bignell CM, Hibbert DB (1997) Use of gas chromatograms of the essential leaf oils of the genus Eucalyptus for taxonomic purposes. Australian Journal of Botany 45, 1–13.
Use of gas chromatograms of the essential leaf oils of the genus Eucalyptus for taxonomic purposes.Crossref | GoogleScholarGoogle Scholar |

Faure R, Ramanoelina ARP, Rakotonirainy O, Bianchini Jp, Gaydou EM (1991) Two-dimensional nuclear magnetic resonance of sesquiterpenes. 4: application to complete assignment of 1 H and 13 C NMR spectra of some aromadendrane derivatives. Magnetic Resonance in Chemistry 29, 969–971.
Two-dimensional nuclear magnetic resonance of sesquiterpenes. 4: application to complete assignment of 1 H and 13 C NMR spectra of some aromadendrane derivatives.Crossref | GoogleScholarGoogle Scholar |

Grayling PM, Brooker MIH (1996) Evidence for the identity of the hybrid, Eucalyptus ‘brachyphylla’ (Myrtaceae) from morphology and essential-oil composition. Australian Journal of Botany 44, 1–13.
Evidence for the identity of the hybrid, Eucalyptus ‘brachyphylla’ (Myrtaceae) from morphology and essential-oil composition.Crossref | GoogleScholarGoogle Scholar |

Guenther E (1948) ‘The Essential Oils: History – Origin in Plants – Production – Analysis.’ (Van Nostrand: New York, NY, USA)

Harley RM, Bell MG (1967) Taxonomic analysis of herbarium material by gas chromatography. Nature 213, 1241–1242.
Taxonomic analysis of herbarium material by gas chromatography.Crossref | GoogleScholarGoogle Scholar |

Hartmann T (2007) From waste products to ecochemicals: fifty years research of plant secondary metabolism. Phytochemistry 68, 2831–2846.
From waste products to ecochemicals: fifty years research of plant secondary metabolism.Crossref | GoogleScholarGoogle Scholar |

Jarmusch AK, Cooks RG (2014) Emerging capabilities of mass spectrometry for natural products. Natural Product Reports 31, 730–738.
Emerging capabilities of mass spectrometry for natural products.Crossref | GoogleScholarGoogle Scholar |

Jautelat M, Grutzner JB, Roberts JD (1970) Natural-abundance 13C nuclear magnetic resonance spectra of terpenes and carotenes. Proceedings of the National Academy of Sciences of the United States of America 65, 288–292.
Natural-abundance 13C nuclear magnetic resonance spectra of terpenes and carotenes.Crossref | GoogleScholarGoogle Scholar |

Keefover-Ring K, Thompson JD, Linhart YB (2009) Beyond six scents: defining a seventh Thymus vulgaris chemotype new to southern France by ethanol extraction. Flavour and Fragrance Journal 24, 117–122.
Beyond six scents: defining a seventh Thymus vulgaris chemotype new to southern France by ethanol extraction.Crossref | GoogleScholarGoogle Scholar |

Kennington WJ (2009) Volatile leaf oil diversity in the narrow range endemic Eucalyptus argutifolia (Myrtaceae) and its widespread congener Eucalyptus obtusiflora. Biological Journal of the Linnean Society. Linnean Society of London 96, 738–745.
Volatile leaf oil diversity in the narrow range endemic Eucalyptus argutifolia (Myrtaceae) and its widespread congener Eucalyptus obtusiflora.Crossref | GoogleScholarGoogle Scholar |

King DJ, Gleadow RM, Woodrow IE (2006) Regulation of oil accumulation in single glands of Eucalyptus polybractea. New Phytologist 172, 440–451.
Regulation of oil accumulation in single glands of Eucalyptus polybractea.Crossref | GoogleScholarGoogle Scholar |

Liu J, Wang H, Cooks RG, Ouyang Z (2011) Leaf spray: direct chemical analysis of plant material and living plants by mass spectrometry. Analytical Chemistry 83, 7608–7613.
Leaf spray: direct chemical analysis of plant material and living plants by mass spectrometry.Crossref | GoogleScholarGoogle Scholar |

Lowe RF, Russell MF, Southwell IA, Day J (2005) Astartea, a new source of (+)-(1S, 5R)-myrtenal. The Journal of Essential Oil Research 17, 683–685.
Astartea, a new source of (+)-(1S, 5R)-myrtenal.Crossref | GoogleScholarGoogle Scholar |

Phillipson JD (1982) Chemical investigations of herbarium material for alkaloids. Phytochemistry 21, 2441–2456.
Chemical investigations of herbarium material for alkaloids.Crossref | GoogleScholarGoogle Scholar |

Raffauf RF, Morris EA (1960) Persistence of alkaloids in plant tissue. Science 131, 1047
Persistence of alkaloids in plant tissue.Crossref | GoogleScholarGoogle Scholar |

Schwab NV, Eberlin MN (2013) Mass spectrometry made easy: the quest for simplicity. Drug Testing and Analysis 5, 137–144.
Mass spectrometry made easy: the quest for simplicity.Crossref | GoogleScholarGoogle Scholar |

Sharma G (2013) Role of phytochemicals and nucleic acids in solving taxonomic problems. Proceedings of the National Academy of Sciences. India – B. Biological Sciences 83, 141–145.
Role of phytochemicals and nucleic acids in solving taxonomic problems.Crossref | GoogleScholarGoogle Scholar |

Sokal RR, Rohlf FJ (1995) ‘Biometry: the Principles and Practice of Statistics in Biological Research.’ (Ed. FJ Rohlf) (W.H. Freeman: New York, NY, USA)

Southwell IA, Stiff IA (1989) Ontogenetical changes in monoterpenoids of Melaleuca alternifolia leaf. Phytochemistry 28, 1047–1051.
Ontogenetical changes in monoterpenoids of Melaleuca alternifolia leaf.Crossref | GoogleScholarGoogle Scholar |

Stuessy TF (2009) ‘Plant Taxonomy: the Systematic Evaluation of Comparative Data.’ (Columbia University Press: New York, NY, USA)

Telford I, Bruhl J (2014) Phebalium verrucosum (Rutaceae: Boronieae), new status for a taxon excluded from P. squamulosum on morphological and phytochemical evidence. Telopea 16, 127–132.
Phebalium verrucosum (Rutaceae: Boronieae), new status for a taxon excluded from P. squamulosum on morphological and phytochemical evidence.Crossref | GoogleScholarGoogle Scholar |

Unger J, Merhof D, Renner S (2016) Computer vision applied to herbarium specimens of German trees: testing the future utility of the millions of herbarium specimen images for automated identification. BMC Evolutionary Biology 16, 248–254.
Computer vision applied to herbarium specimens of German trees: testing the future utility of the millions of herbarium specimen images for automated identification.Crossref | GoogleScholarGoogle Scholar |

Wallis IR, Foley WJ (2005) The rapid determination of sideroxylonals in Eucalyptus foliage by extraction with sonication followed by HPLC. Phytochemical Analysis 16, 49–54.
The rapid determination of sideroxylonals in Eucalyptus foliage by extraction with sonication followed by HPLC.Crossref | GoogleScholarGoogle Scholar |

Wenig P, Odermatt J (2010) OpenChrom: a cross-platform open source software for the mass spectrometric analysis of chromatographic data. BMC Bioinformatics 11, 405–413.
OpenChrom: a cross-platform open source software for the mass spectrometric analysis of chromatographic data.Crossref | GoogleScholarGoogle Scholar |

Wink M (2003) Evolution of secondary metabolites from an ecological and molecular phylogenetic perspective. Phytochemistry 64, 3–19.
Evolution of secondary metabolites from an ecological and molecular phylogenetic perspective.Crossref | GoogleScholarGoogle Scholar |